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Perinatal Research Laboratories, Harbor-UCLA Medical Center, University of California, Los Angeles, School of Medicine, Torrance, California 90502
Received 10 September 1996; accepted in final form 12 March 1997.
Rebello, Celso M., Machiko Ikegami, M. Gore Ervin, Daniel H. Polk, and Alan H. Jobe. Postnatal lung function and protein permeability after fetal or maternal corticosteroids in preterm lambs.
J. Appl. Physiol. 83(1): 213-218, 1997.
We evaluated postnatal lung function and
intravascular albumin loss to tissues of 123-days-gestation preterm
surfactant-treated and ventilated lambs 15 h after direct fetal
(n = 8) or maternal
(n = 9) betamethasone treatment or
saline placebo (n = 9). The
betamethasone-treated groups had similar increases in dynamic
compliances, ventilatory efficiency indexes, and lung volumes relative
to controls (P < 0.05). The losses
of 125I-labeled albumin from
blood, a marker of intravascular integrity, and the recoveries of
125I-albumin in muscle and brain
were similar for control and betamethasone-exposed lambs.
Betamethasone-treated lambs had lower recoveries of
125I-albumin in lung tissues and
in alveolar washes than did controls (P < 0.01). Although blood pressures
were higher for the treated groups (P < 0.05), all groups had similar blood volumes, cardiac outputs, and
organ blood flows. Maternal or fetal treatment with betamethasone 15 h
before preterm delivery equivalently improved postnatal lung function,
reduced albumin recoveries in lungs, and increased blood pressures.
However, prenatal betamethasone had no effects on the systemic
intravascular losses of albumin or did not change blood volumes.
respiratory distress syndrome; edema; fetal therapy; lung maturation
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